Search research articles
Contact Us
Filters
Showing results (61-70 of 93) with videos related to
Page
of 10
Sort By:
Medchemcomm
|
August 16, 2018
Discovery and biological evaluation of N5-substituted 6,7-dioxo-6,7-dihydropteridine derivatives as potent Bruton's tyrosine kinase inhibitors
Haiyang Chen, Peiran Song, Yanyan Diao, et al.
International Journal of Molecular Medicine
|
November 3, 2018
Resveratrol suppresses colon cancer growth by targeting the AKT/STAT3 signaling pathway
Dan Li, Gangcheng Wang, Guoguo Jin, et al.
Journal of Medicinal Chemistry
|
June 16, 2018
Design, Synthesis, and Biological Evaluation of Pyrimido[4,5- d]pyrimidine-2,4(1 H,3 H)-diones as Potent and Selective Epidermal Growth Factor Receptor (EGFR) Inhibitors against L858R/T790M Resistance Mutation
Yongjia Hao, Jiankun Lyu, Rong Qu, et al.
Journal of Medicinal Chemistry
|
April 17, 2026
Rational Design, Synthesis, and Biological Evaluation of Potent, Highly Selective 1,2,4-Oxadiazole-Based S1PR1 Agonists for UC Treatment
Tianyu Ye, Yunping Xiao, Chenyang Tang, et al.
Communications Chemistry
|
October 7, 2025
Exploring the macrocyclic chemical space for heuristic drug design with deep learning models
Feng Hu, Xiaotong Jia, Wenjie Liao, et al.
Journal of Medicinal Chemistry
|
August 28, 2025
Direct Ser797 Interacted Pteridine-7(8<i>H</i>)-one Derivatives as Highly Selective and Orally Available EGFR<sup>L858R/T790M/C797S</sup> Inhibitors
Wenzhe Jiang, Yupei He, Yongxiang Wang, et al.
Biochemical Pharmacology
|
April 18, 2026
Discovery of novel CSF1R inhibitor for triple-negative breast cancer (TNBC) treatment through TAMs reprogramming
Wenjie Sha, Zitong Yan, Yunpeng Wu, et al.
Journal of Medicinal Chemistry
|
April 7, 2025
Design, Synthesis, and Biological Evaluation of Pyrrolo[1,2-<i>a</i>]quinoxalin-4(5<i>H</i>)-one Derivatives as Potent and Orally Available Noncovalent Bruton's Tyrosine Kinase (BTK) Inhibitors
Chaoquan Tian, Husheng Du, Wenjie Sha, et al.
International Journal of Molecular Sciences
|
January 11, 2024
Binding Free Energy Calculation Based on the Fragment Molecular Orbital Method and Its Application in Designing Novel SHP-2 Allosteric Inhibitors
Zhen Yuan, Xingyu Chen, Sisi Fan, et al.
Journal of Medicinal Chemistry
|
July 12, 2016
Discovery and Structural Optimization of N5-Substituted 6,7-Dioxo-6,7-dihydropteridines as Potent and Selective Epidermal Growth Factor Receptor (EGFR) Inhibitors against L858R/T790M Resistance Mutation
Yongjia Hao, Xia Wang, Tao Zhang, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 93) with videos related to
Sort By:
Page
of 10
Medchemcomm
|
August 16, 2018
Discovery and biological evaluation of N5-substituted 6,7-dioxo-6,7-dihydropteridine derivatives as potent Bruton's tyrosine kinase inhibitors
Haiyang Chen, Peiran Song, Yanyan Diao, et al.
International Journal of Molecular Medicine
|
November 3, 2018
Resveratrol suppresses colon cancer growth by targeting the AKT/STAT3 signaling pathway
Dan Li, Gangcheng Wang, Guoguo Jin, et al.
Journal of Medicinal Chemistry
|
June 16, 2018
Design, Synthesis, and Biological Evaluation of Pyrimido[4,5- d]pyrimidine-2,4(1 H,3 H)-diones as Potent and Selective Epidermal Growth Factor Receptor (EGFR) Inhibitors against L858R/T790M Resistance Mutation
Yongjia Hao, Jiankun Lyu, Rong Qu, et al.
Journal of Medicinal Chemistry
|
April 17, 2026
Rational Design, Synthesis, and Biological Evaluation of Potent, Highly Selective 1,2,4-Oxadiazole-Based S1PR1 Agonists for UC Treatment
Tianyu Ye, Yunping Xiao, Chenyang Tang, et al.
Communications Chemistry
|
October 7, 2025
Exploring the macrocyclic chemical space for heuristic drug design with deep learning models
Feng Hu, Xiaotong Jia, Wenjie Liao, et al.
Journal of Medicinal Chemistry
|
August 28, 2025
Direct Ser797 Interacted Pteridine-7(8<i>H</i>)-one Derivatives as Highly Selective and Orally Available EGFR<sup>L858R/T790M/C797S</sup> Inhibitors
Wenzhe Jiang, Yupei He, Yongxiang Wang, et al.
Biochemical Pharmacology
|
April 18, 2026
Discovery of novel CSF1R inhibitor for triple-negative breast cancer (TNBC) treatment through TAMs reprogramming
Wenjie Sha, Zitong Yan, Yunpeng Wu, et al.
Journal of Medicinal Chemistry
|
April 7, 2025
Design, Synthesis, and Biological Evaluation of Pyrrolo[1,2-<i>a</i>]quinoxalin-4(5<i>H</i>)-one Derivatives as Potent and Orally Available Noncovalent Bruton's Tyrosine Kinase (BTK) Inhibitors
Chaoquan Tian, Husheng Du, Wenjie Sha, et al.
International Journal of Molecular Sciences
|
January 11, 2024
Binding Free Energy Calculation Based on the Fragment Molecular Orbital Method and Its Application in Designing Novel SHP-2 Allosteric Inhibitors
Zhen Yuan, Xingyu Chen, Sisi Fan, et al.
Journal of Medicinal Chemistry
|
July 12, 2016
Discovery and Structural Optimization of N5-Substituted 6,7-Dioxo-6,7-dihydropteridines as Potent and Selective Epidermal Growth Factor Receptor (EGFR) Inhibitors against L858R/T790M Resistance Mutation
Yongjia Hao, Xia Wang, Tao Zhang, et al.
Page
of 10